Dr Marvel Anti Dandruff Scalp Serum Solution
NDC Package 87770-025-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Dr Marvel Anti Dandruff Scalp Serum (selenium sulfide salicylic acid) solution is apply to affected areas one to fourimes daily or as directed by doctor Shake before use Apply 2 to 3 drops inargeted areas directly to wet or dryscalp. This formulation utilizes a solution delivery system. Marketed by Guangzhou Liyan Cosmetics Technology Co., Ltd., this product is identified by NDC 87770-025 and is authorized under FDA application M032.

Identification & Billing

NDC Package Code
87770-025-01
Package Description
100 mg in 1 BOX
Product Code
87770-025
11-Digit Billing Format
87770002501

Clinical Specifications

Proprietary Name
Dr Marvel Anti Dandruff Scalp Serum
Non-Proprietary Name
Selenium Sulfide Salicylic Acid
Substance Name
Salicylic Acid; Selenium Sulfide
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
Usage Information
Apply to affected areas one to fourimes daily or as directed by doctor Shake before use Apply 2 to 3 drops inargeted areas directly to wet or dryscalp. Gently massage in. Use more asneeded. Apply to skin, leave on for15-20 minutes, then rinse off.

Regulatory & Marketing

Labeler Name
Guangzhou Liyan Cosmetics Technology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M032
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-05-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 87770-025-01 identifies a specific commercial package of 100 mg in 1 box of Dr Marvel Anti Dandruff Scalp Serum, a human over the counter drug labeled by Guangzhou Liyan Cosmetics Technology Co., Ltd.. This solution is formulated for topical use and contains salicylic acid; selenium sulfide as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Guangzhou Liyan Cosmetics Technology Co., Ltd. on September 05, 2026. The current certification is valid through December 31, 2027.

How is this Guangzhou Liyan Cosmetics Technology Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87770002501. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
87770-025-01
11-Digit CMS (5-4-2)
87770-0025-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.